552313
4-苯基苄胺
97%
别名:
(4-Phenylphenyl)methanamine, 1-(Biphenyl-4-yl)methanamine, 4-(Aminomethyl)biphenyl, 4-Biphenylmethylamine, Biphenyl-4-ylmethanamine, [(1,1′-Biphenyl-4-yl)methyl]amine, [(Biphenyl-4-yl)methyl]amine, [1,1′-Biphenyl]-4-ylmethanamine, p-Phenylbenzylamine
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关于此项目
线性分子式:
C6H5C6H4CH2NH2
化学文摘社编号:
分子量:
183.25
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
InChI
1S/C13H13N/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9H,10,14H2
SMILES string
NCc1ccc(cc1)-c2ccccc2
InChI key
RMSPOVPGDBDYKH-UHFFFAOYSA-N
assay
97%
mp
48-53 °C (lit.)
functional group
amine, phenyl
Other Notes
在氮气下处理和储存，以抑制杂质的形成。
Application
4-Phenylbenzylamine may be used in the synthesis of:
4-Phenylbenzylamine may also be used in the synthesis of Gd3+ chelates of DOTA(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate) type ligands.
- squaric acid asymmetric diamides of glycopeptide antibiotics
- asymmetric diamides of daunomycin and carminomycin
- N-(biphenyl-4-ylmethyl)-1-hydroxy-6-thioxo-1,6-dihydropyridine-2-carboxamide
4-Phenylbenzylamine may also be used in the synthesis of Gd3+ chelates of DOTA(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate) type ligands.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
A new series of glycopeptide antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 59(9), 564-564 (2006)
chemical society(Great Britain)
Journal of the Chemical Society, Part 1 (1993)
A new class of semisynthetic anthracycline glycoside antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 58(11), 704-704 (2005)
Coupling fast water exchange to slow molecular tumbling in Gd3+ chelates: why faster is not always better.
Avedano S, et al.
Inorganic Chemistry, 52(15), 8436-8450 (2013)
Thioamide hydroxypyrothiones supersede amide hydroxypyrothiones in potency against anthrax lethal factor.
Agrawal A, et al.
Journal of Medicinal Chemistry, 52(4), 1063-1074 (2009)
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